
Help Me Bring PFS Awareness to the World Congress of Hair Restoration Surgery
I’m currently in discussions with a representative from the International Society of Hair Restoration Surgery (ISHRS) about potentially sharing my PFS story at their World Congress in Rio de Janeiro this October 2026.
I need your help to show them that this issue extends far beyond one person.
If you’re suffering from PFS and are willing to share your experience, please record a short, approximately one-minute YouTube video covering:
- Your first name, age, and general location
- The medication you took before developing PFS
- When and how your symptoms began
- Your past and current symptoms
- Treatments or medications you’ve tried since
- End with: “I wish I had never taken this drug.”
Here is my video as an example:
Once your video is posted, send me the YouTube link. I plan to compile the videos and share them with the World Congress contact I’ve been corresponding with.
My goal is to demonstrate that people around the world are reporting persistent, life-altering symptoms after using finasteride or related medications, and that patients deserve to be heard by the physicians who prescribe these drugs.
A strong response from this community could help make the case for giving PFS patients a voice at the Congress.
If you’ve ever wanted an opportunity to make your story heard, this is one. Please record a video, post it, and send me the link. Every voice helps.